A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv893561



Internal ID15840831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:11930721..11934079hg38UCSC Ensembl
Innerchr19:12041536..12044894hg19UCSC Ensembl
Innerchr19:11902536..11905894hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg383359
hg193359
hg183359
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578623
Supporting Variants
Samples
Known GenesZNF700
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv893561
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer